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Allele : Hcn2<trls> hyperpolarization-activated, cyclic nucleotide-gated K+ 2; tremor and reduced lifespan
Primary Identifier  MGI:3582957 Allele Type  Spontaneous
Gene  Hcn2 Inheritance Mode  Recessive
Strain of Origin  BKS.Cg-Dock7<m> +/+ Lepr<db>/J Is Recombinase  false
Is Wild Type  false
molecularNote  This spontaneous mutation has a G-to-A transition at chromosome 10 position 79,724,780 (GRCm38) that causes an arginine to glutamine substitution at residue 315 (p.R315Q).
  • mutations:
  • Single point mutation
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1 Feature

Trail: Allele

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

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Trail: Allele




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